Materials for organic electroluminescent devices

ABSTRACT

The present invention relates to coordination compounds which are used in an electron-transport layer in electronic devices, to ligands, and to the use thereof for the preparation of metal complexes, to a layer, and to an electronic device which comprise the compounds according to the invention, and to a process for the preparation of the compounds according to the invention.

The present invention relates to coordination compounds of the generalformulae (1) to (21), in particular as materials in theelectron-transport layer in electronic devices, to ligands of thegeneral formula (1′), to a process for the preparation thereof, and tothe use thereof for the preparation of a metal complex, to a layer, andto an electronic device which comprise the compounds according to theinvention.

Chelate complexes and organometallic compounds are used as functionalmaterials in a number of different applications which can be ascribed tothe electronics industry in the broadest sense. In spite of thesuccesses that have already been achieved, further improvements arestill desirable in the case of the organic electroluminescent devicesbased on organic components (general description of the structure cf.U.S. Pat. No. 4,539,507 and U.S. Pat. No. 5,151,629) and the individualcomponents thereof, the organic light-emitting diodes (OLEDs).

There is also a need for improvement in the case of, in particular, theelectron-transport materials used hitherto with respect to theirlifetime and efficiency. A further requirement of materials used inOLEDs is that they have a high degree of purity. A high glass transitiontemperature of these compounds and a low tendency towardscrystallisation are highly desired. Furthermore, there is a need forimprovement in the case of materials which are processed from solution.

At present, a large number of electron-transport materials is available.Thus, for example, WO 2003/060956 describes 9,10-diarylanthracenederivatives which carry a benzimidazole group in the structure aselectron-transport materials. In addition, 8-hydroxyquinoline-metalcomplexes, whose influence on emission spectra has been studied bychanging the substitution pattern, are known, for example, from Chem.Eur. J. 2006, 12, 4523.

Frequently, either an electron-transport layer and an adjacentelectron-injection layer are used on the cathode side of an OLED, or amixture of an electron-transport material and an electron-injectionmaterial is used in a layer. The electron-injection materials used hereinclude, inter alia, metal complexes, such as, for example, Liq (lithiumquinolinate). It would be desirable if it were possible to use only onelayer consisting of one material here instead of using two materials ina mixture or in successive layers. This would simplify production andenable better process control since vapour deposition does not have tobe carried out from two sources.

There is therefore a need for novel compounds which have improvedproperties, in particular with respect to the above-mentioned problems.The object of the invention thus consisted in the provision of suchcompounds.

Surprisingly, it has been found that complexes containinghydroxyquinoline derivatives as ligands which contain anelectron-deficient heteroaryl group covalently bonded via an aromaticsystem achieve a long operating lifetime and/or high stability totemperature stresses compared with the compounds already presented inthe prior art. The said compounds can furthermore be processed well fromsolution and can be employed in an OLED without the use of a separateelectron-injection layer.

In order to achieve the said object, the present invention provides acompound of the general formula (1) or (2):

The symbols and indices used in formula (1) or (2) have the followingmeanings:

-   G is, identically or differently on each occurrence, a group of the    following formula (a), (b) or (c):

-   Q is selected, identically or differently on each occurrence, from    the group consisting of N and CR³;-   V is selected from the group consisting of O, S, N, CR⁴ and NR⁴,    with the proviso that, if V is equal to O, S or NR⁴, R³ represents a    non-bonding electron pair;    the two dashed bonds in formula (a) and (b) mean that one of the    bonds is a single covalent bond and the other is a double covalent    bond;-   R¹ is selected, identically or differently on each occurrence, from    the group defined for R², R³ or R⁴; where one R¹ is not present, and    the quinoline unit is bonded to Y² at this position;-   R², R³, R⁴ are selected, identically or differently on each    occurrence, from the group consisting of H, D, F, Cl, Br, I, CHO,    N(Ar¹)₂, C(═O)Ar¹, P(═O)(Ar¹)₂, S(═O)Ar¹, S(═O)₂Ar¹, OR⁵═OR⁵Ar¹, CN,    NO₂, Si(R⁵)₃, B(OAr¹)₂, B(OR⁵)₂, OSO₂R⁵, OH, a saturated or    unsaturated, straight-chain, branched or cyclic C₁₋₄₀-alkyl group,    C₁₋₄₀-alkoxy group or C₁₋₄₀-thioalkyl group, each of which may be    substituted by one or more radicals R⁵, where one or more    non-adjacent CH₂ groups may be replaced by R⁵C═CR⁵, C≡O, Si(R⁵)₂,    Ge(R⁵)₂, Sn(R⁵)₂, C═O, C═S, C═Se, C═NR⁵, P(═O)(R⁵), SO, SO₂, NR⁵, O,    S or CONR⁵, and where one or more H atoms may be replaced by D, F,    Cl, Br, I, CN or NO₂, an aromatic or heteroaromatic ring system    having 5 to 60 aromatic ring atoms, which may be substituted by one    or more radicals R⁶, an aryl-oxy or heteroaryloxy group having 5 to    60 aromatic ring atoms, which may be substituted by one or more    radicals R⁶, and a combination of these systems; where one of the    substituents R², R³ or R⁴ is not present on the group G, and the    group G is bonded to Y¹ at this position;-   W is selected, identically or differently on each occurrence, from    O, S and NR⁸, where R⁸ is selected from the group defined for R², R³    or R⁴;-   Y¹, Y² are each, independently of one another, either not present,    so that the groups bonded thereto are linked directly to one another    by a single covalent bond, or are selected from the group consisting    of a saturated or unsaturated, linear, branched or cyclic    C₁₋₄₀-alkyl group and an aromatic or heteroaromatic ring system    having 5 to 60 ring atoms, which may be substituted by one or more    radicals R⁶;-   Ar is an aromatic or heteroaromatic ring system having 5 to 60    aromatic ring atoms, which may be substituted by one or more    radicals R⁹, where R⁹ is selected from the group defined for R², R³    or R⁴;-   Ar¹ is, identically or differently on each occurrence, an aromatic    or hetero-aromatic ring system having 5 to 30 aromatic ring atoms,    which may be substituted by one or more radicals R⁷, where, in    addition, two radicals Ar¹ which are bonded to the same nitrogen or    phosphorus atom may be linked to one another by a single bond or a    bridge selected from B(R⁷), C(R⁷)₂, Si(R⁷)₂, C═O, C═NR⁷, C═C(R⁷)₂,    O, S, S═O, SO₂, N(R), P(R⁷) and P(═O)R⁷;-   R⁵ is selected, identically or differently on each occurrence, from    the group consisting of H, D, a saturated or unsaturated, linear,    branched or cyclic C₁₋₂₀-alkyl group, in which one or more H atoms    may be replaced by D or F, and an aromatic or heteroaromatic ring    system having 5 to 20 ring atoms, in which one or more H atoms may    be replaced by F, and which may be substituted by one or more    radicals R⁶;-   R⁶ is selected, identically or differently on each occurrence, from    the group consisting of H, D, F, Cl, Br, I, CHO, N(Ar¹)₂, C(═O)Ar¹,    P(═O)(Ar¹)₂, S(═O)Ar¹, S(═O)₂Ar¹, CR⁷═CR⁷Ar¹, CN, NO₂, Si(R⁷)₃,    B(OAr¹)₂, B(OR⁷)₂, OSO₂R⁷, OH, and a saturated or unsaturated,    straight-chain, branched or cyclic C₁₋₄₀-alkyl group, C₁₋₄₀-alkoxy    group or C₁₋₄₀-thioalkyl group, each of which may be substituted by    one or more radicals R⁷, where one or more non-adjacent CH₂ groups    may be replaced by R⁷C═CR⁷, C≡C, Si(R⁷)₂, Ge(R⁷)₂, Sn(R⁷)₂, C═O,    C═S, C═Se, C═NR⁷, P(═O)(R⁷), SO, SO₂, NR⁷, O, S or CONR⁷, and where    one or more H atoms may be replaced by D, F, Cl, Br, I, CN or NO₂,-   R⁷ is selected, identically or differently on each occurrence, from    the group consisting of H, D, a saturated or unsaturated, linear,    branched or cyclic C₁₋₂₀-alkyl group, in which one or more H atoms    may be replaced by F or D, and an aromatic or heteroaromatic ring    system having 5 to 20 ring atoms, in which one or more H atoms may    be replaced by F or D;-   M is, identically or differently on each occurrence, a mono-, di-,    tri- or tetravalent metal;-   L′ is, identically or differently on each occurrence, a monodentate    or bidentate ligand;-   m is, identically or differently on each occurrence, 0, 1, 2, 3 or    4, with the proviso that at least one index m is >0;-   n is 1, 2, 3 or 4;-   r is 1, 2, 3 or 4;-   k is, identically or differently on each occurrence, 0, 1, 2, 3, 4,    5 or 6; and-   l is 0, 1, 2, 3, 4, 5 or 6.

The following general definitions are used within this invention:

For the purposes of the present invention, a saturated or unsaturated,straight-chain, branched or cyclic C₁₋₂₀-alkyl group or C₁₋₄₀-alkylgroup is taken to mean an alkyl, alkenyl and alkynyl groups having 1 to20 or 1 to 40 C atoms respectively. Individual —CH— or —CH₂— groups maybe substituted by N, NH, O or S. Preference is given to the radicalsmethyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, s-butyl, t-butyl,2-methylbutyl, n-pentyl, s-pentyl, neopentyl, cyclopentyl, n-hexyl,cyclohexyl, neohexyl, n-heptyl, cycloheptyl, n-octyl, cyclooctyl,2-ethylhexyl, trifluoromethyl, pentafluoro-ethyl, 2,2,2-trifluoroethyl,ethenyl, propenyl, butenyl, pentenyl, cyclo-pentenyl, hexenyl,cyclohexenyl, heptenyl, cycloheptenyl, octenyl, cyclo-octenyl, ethynyl,propynyl, butynyl, pentynyl, hexynyl, heptynyl or octynyl. Particularpreference is given to alkyl groups having 1 to 6 carbon atoms, evenmore preferably having 1 to 4 carbon atoms, in particular methyl andtert-butyl.

Aliphatic hydrocarbons having 1 to 20 carbon atoms are linear, branchedor cyclic alkyl groups, alkenyl groups, alkynyl groups, in which one ormore carbon atoms may be replaced by O, N or S. In addition, one or morehydrogen atoms may be replaced by fluorine. Examples of aliphatichydro-carbons having 1 to 20 carbon atoms include the same ones asdefined above for the alkyl, alkenyl and alkynyl groups.

A C₁₋₄₀-alkoxy group or C₁₋₄₀-thioalkyl group is taken to mean aC₁₋₄₀-alkyl group as defined above which is bonded via an O or S atom.Preference is given to alkoxy groups having 1 to 20 carbon atoms,particularly preferably 1 to 6 carbon atoms, extraordinarily preferably1 to 4 carbon atoms.

The alkyl groups, alkoxy groups and thioalkyl groups may, in addition,be substituted by one or more radicals R⁵ as defined above.

An aromatic or heteroaromatic ring system having 5 to 60, or 5 to 30ring atoms, or 5 to 20 ring atoms in the sense of this invention istaken to mean an aromatic ring system having 6 to 60, or 6 to 30, or 6to 20 carbon atoms respectively, or a heteroaromatic ring system having5 to 60, or 5 to 30, or 5 to 20 carbon atoms respectively, one or morecarbon atoms of which may be substituted by a heteroatom. Preferredheteroatoms are N, O and S. These aromatic ring systems may bemonocyclic or polycyclic, i.e. they may have one ring (for examplephenyl) or two or more rings (for example biphenyl, fluorenyl), whichmay also be in condensed form (for example naphthyl).

Preference is given to aromatic or heteroaromatic ring systems having 5to 30 aromatic ring atoms, particularly preferably 5 to 24 aromatic ringatoms, more preferably 5 to 14 aromatic ring atoms. Preferred aromaticring systems having 6 to 60, or 6 to 30, or 6 to 24 carbon atomsrespectively are, for example, phenyl, naphthalene, anthracene,benzanthracene, phenanthrene, benzophenanthrene, pyrene, benzopyrene,chrysene, perylene, biphenyl, terphenyl, fluorene, spirobifluorene,indene, indenofluorene, benzindenofluorene, dibenzindenofluorene orfluoranthene.

Preferred heteroaromatic ring systems having 5 to 60, or 5 to 30, or 5to 24 ring atoms respectively are, for example, 5-membered rings, suchas pyrrole, pyrazole, imidazole, 1,2,3-triazole, 1,2,4-triazole,tetrazole, furan, thiophene, selenophene, oxazole, isoxazole,1,2-thiazole, 1,3-thiazole, 1,2,3-oxadiazole, 1,2,4-oxadiazole,1,2,5-oxadiazole, 1,3,4-oxadiazole, 1,2,3-thiadiazole,1,2,4-thiadiazole, 1,2,5-thiadiazole, 1,3,4-thiadiazole, 6-memberedrings, such as pyridine, pyridazine, pyrimidine, pyrazine,1,3,5-triazine, 1,2,4-triazine, 1,2,3-triazine, 1,2,4,5-tetrazine,1,2,3,4-tetrazine, 1,2,3,5-tetrazine, or condensed groups, such asindole, isoindole, indolizine, indazole, benzimidazole, benzotriazole,purine, naphthimidazole, phenanthrimidazole, pyridimidazole,pyrazinimidazole, quinoxalin-imidazole, benzoxazole, naphthoxazole,anthroxazole, phenanthroxazole, isoxazole, benzothiazole, benzofuran,isobenzofuran, dibenzofuran, quinoline, isoquinoline, pteridine,benzo-5,6-quinoline, benzo-6,7-quinoline, benzo-7,8-quinoline,benzoisoquinoline, acridine, phenothiazine, phenoxazine,benzopyridazine, benzopyrimidine, quinoxaline, phenazine, naphthyridine,azacarbazole, benzocarboline, phenanthridine, phenanthroline,thieno[2,3b]thiophene, thieno[3,2b]thiophene, dithienothiophene,isobenzothiophene, dibenzothiophene, benzothiadiazothiophene, orcombinations of these groups. Particular preference is given toimidazole, benzimidazole, pyridine, pyrimidine and triazine

The mono- or polycyclic aromatic or heteroaromatic ring systems having 5to 60 ring atoms may carry one or more substituents which are definedabove under R⁶.

An aryloxy or heteroaryloxy group having 5 to 60 aromatic ring atoms istaken to mean a group which carries a mono- or polycyclic aromatic orheteroaromatic ring system having 5 to 60 ring atoms as defined abovevia an O atom. Preference is given to aryloxy or heteroaryloxy groupshaving 5 to 30 aromatic ring atoms, particularly preferably 5 to 20 ringatoms, more preferably 5 to 10 ring atoms. The aryloxy or heteroaryloxygroup may likewise carry one or more substituents which are definedabove under R⁶.

M is preferably an element, a metal or a metal ion selected from thegroup consisting of alkali metal, alkaline-earth metal, boron group andsub-group elements. M is particularly preferably a metal or a metal ionof an element selected from the group consisting of Li, Be, Ca, Mg, Ba,Zn, B, Al, Zr, Cu, Sc and Y, extraordinarily preferably Li, Ca, Mg, Zn,Al and Zr.

The following applies to compounds of the formula (1) which arepreferred in accordance with the invention:

If M is a metal having two coordination sites, then k is equal to 0;

if M is a metal having three coordination sites and L′ is a monodentateligand, then k is equal to 1;if M is a metal having four coordination sites and L′ is a monodentateligand, then k is equal to 2;if M is a metal having five coordination sites and L′ is a monodentateligand, then k is equal to 3;if M is a metal having six coordination sites and L′ is a monodentateligand, then k is equal to 4;if M is a metal having seven coordination sites and L′ is a monodentateligand, then k is equal to 5;if M is a metal having eight coordination sites and L′ is a monodentateligand, then k is equal to 6;if M is a metal having four coordination sites and L′ is a bidentateligand, then k is equal to 1;if M is a metal having six coordination sites and L′ is a bidentateligand, then k is equal to 2;if M is a metal having eight coordination sites and L′ is a bidentateligand, then k is equal to 3.

The following applies to compounds of the formula II which are preferredin accordance with the invention:

if M is a metal having two coordination sites and r is equal to 1, thenl is equal to 0;if M is a metal having three coordination sites, U is a monodentateligand and r is equal to 1, then l is equal to 1;if M is a metal having four coordination sites, L′ is a monodentateligand and r is equal to 1, then l is equal to 2;if M is a metal having five coordination sites, L′ is a monodentateligand and r is equal to 1, then l is equal to 3;if M is a metal having six coordination sites, L′ is a monodentateligand and r is equal to 1, then l is equal to 4;if M is a metal having seven coordination sites, L′ is a monodentateligand and r is equal to 1, then l is equal to 5;if M is a metal having eight coordination sites, L′ is a monodentateligand and r is equal to 1, then l is equal to 6;if M is a metal having four coordination sites and r is equal to 2, thenl is equal to 0;if M is a metal having five coordination sites, L′ is a monodentateligand and r is equal to 2, then l is equal to 1;if M is a metal having six coordination sites, L′ is a monodentateligand and r is equal to 2, then l is equal to 2;if M is a metal having seven coordination sites, L′ is a monodentateligand and r is equal to 2, then l is equal to 3;if M is a metal having eight coordination sites, L′ is a monodentateligand and r is equal to 2, then l is equal to 4;if M is a metal having six coordination sites and r is equal to 3, thenl is equal to 0;if M is a metal having seven coordination sites, L′ is a monodentateligand and r is equal to 3, then l is equal to 1;if M is a metal having eight coordination sites, L′ is a monodentateligand and r is equal to 3, then l is equal to 2;if M is a metal having eight coordination sites and r is equal to 4,then l is equal to 0;if M is a metal having four coordination sites, L′ is a bidentate ligandand r is equal to 1, then l is equal to 1;if M is a metal having six coordination sites, L′ is a bidentate ligandand r is equal to 1, then l is equal to 2;if M is a metal having eight coordination sites, L′ is a bidentateligand and r is equal to 1, then l is equal to 3;if M is a metal having six coordination sites, L′ is a bidentate ligandand r is equal to 2, then l is equal to 1;if M is a metal having eight coordination sites, L′ is a bidentateligand and r is equal to 2, then l is equal to 2;if M a metal having eight coordination sites, L′ a bidentate ligand andr equal to 3, then l is equal to 1;if M a metal having eight coordination sites, La bidentate ligand and requal to 4, then l is equal to 0.

It is particularly preferred in accordance with the invention for M tobe a metal having two, four or six coordination sites. In anextraordinarily preferred embodiment, M is equal to Li⁺, Al³⁺ or Zr⁴⁺,in particular Li⁺ or Al³⁺.

In a further embodiment of the present invention, it is preferred forthe group Ar to be selected from the following formulae:

These groups may each also be substituted by one or more radicals R⁹.

In a further embodiment of the present invention, it is preferred forthe group G to be selected from the following formulae:

These structures may also be substituted by one or more substituents R²,R³ or R⁴.

In a further embodiment of the present invention, it is preferred forthe groups Y¹ and Y², identically or differently on each occurrence, notto be present or to be selected from the following groups:

These structures may also be substituted by one or more substituents R⁶.

In a further embodiment of the present invention, it is preferred forthe compound of the formula (1) or (2) according to the invention to bea compound of the following formulae (3) to (12):

where the symbols used have the following meanings:

-   Y¹ and Y² have the same meaning as in the above embodiments;-   R¹⁰ is, identically or differently on each occurrence, either H or a    radical of the following formula (d):

-   -   where L′, k and R¹ have the same meanings as in the above        embodiments, with the proviso that one R¹ is not present, and        the compound of the formula (d) is bonded to the compound of the        formula (3) to (12) at this position;

-   R¹¹ is, identically or differently on each occurrence, either H or a    radical of the following formula (e) or (f):

-   -   where V is selected from the group consisting of O, S and NR⁴        and Q is selected from the group consisting of N and CR³, where        at least one Q, preferably at least two Q, stand for N and where        R³ has the same meaning as in the above embodiments;        with the proviso that both at least one R¹⁰ in each formula and        also at least one R¹¹ in each formula is other than H.

In still a further embodiment of the present invention, the compound ofthe above-mentioned formulae is a compound in which Y¹ and Y² is eachnot present or is a p-phenylene unit, V is an —N-Ph radical and R¹ isequal to H or D, with the proviso that either the R¹ which is in theortho position to the metal-coordinated oxygen atom in the compound ofthe formula (d) or the R¹ which is in the para position to themetal-coordinated oxygen atom in the compound of the formula (d) is notpresent, and the compound of the formula (d) is bonded via thisposition.

It is furthermore preferred for two or three symbols Q in the group ofthe formula (f) to stand for N. The group of the formula (f) isparticularly preferably a 1,3,5-triazine.

In a preferred embodiment of the invention, R¹⁰ is selected from thefollowing formulae, where the bond drawn in indicates the position ofthe link to Y²:

Furthermore, m in all embodiments according to the invention ispreferably equal to 1 or 2.

In addition, n in all embodiments according to the invention ispreferably equal to 1, 2 or 3.

The object according to the invention is also achieved by a compound, anoligomer or a polymer which contains a structural unit of the generalformula (13) to (21):

where the symbols Ar, L′, Y¹ and G and the index m have the samemeanings as in the above embodiments, and the other symbols and indiceshave the following meanings:M is a mono-, di-, tri- or tetravalent metal;L is a bidentate ligand of the following formula (g):

-   -   where the bond dash leading away from Y² represents a bond to Ar        in the structural units of the formulae (13) to (21), and the        arrows leading away from W and N represent a coordination bond        to M, and the symbols Y², W and R¹ have the same meanings as        defined in the above claims, where one R¹ is not present and the        quinoline unit is bonded to Y² at this position;        a is 0, 1 or 2;        b is 0 or 1;        with the proviso that the bond dashes leading away from L in the        structural units of the formulae (13) to (21) represent a bond        to M of a further structural unit, and the bond dashes leading        away from M in the structural units of the formulae (13) to (21)        represent a bond to L of a still further structural unit.

“Polymer” is taken to mean a polymeric compound, which preferably have10 to 10000, particularly preferably 20 to 5000 and in particular 50 to2000 structural units (recurring units), i.e. has been built up from acorrespondingly large number of monomers. An “oligomer” is taken tomean, in accordance with the invention, compounds which preferably have2 to 9 recurring units. The branching factor of the polymers here isbetween 0 (linear polymer with no branching points) and 1 (fullybranched dendrimer). I.e. the terms “polymer” and “oligomer” accordinglyalso encompass dendrimers.

The term “dendrimer” in the present application is intended to be takento mean a highly branched compound which is built up from amultifunctional centre (core), to which branched monomers are bonded ina regular structure, giving a tree-like structure. Both the core and themonomers here can adopt any desired branched structures. “Dendrimer”here is generally intended to be understood as described, for example,by M. Fischer and F. Vögtle (Angew. Chem., Int. Ed. 1999, 38, 885).

M in the structural unit of the general formula (13) to (21) ispreferably an element, a metal or a metal ion of an element selectedfrom the group consisting of Ca, Mg, Ba, Zn, B, Al, Zr, Cu, Sc and Y,particularly preferably Ca, Mg, Zn, Al and Zr. Al³⁺ is extraordinarilypreferred.

The following preferably applies to the compound, oligomer or polymer ofthe formulae (13) to (15):

If M is a metal having four coordination sites, then a is equal to 0;

if M is a metal having five coordination sites and L′ is monodentate,then a is equal to 1;if M is a metal having six coordination sites and L′ is monodentate,then a is equal to 2;if M is a metal having seven coordination sites and L′ is monodentate,then a is equal to 3;if M is a metal having eight coordination sites and L′ is monodentate,then a is equal to 4;if M is a metal having six coordination sites and L′ is bidentate, thena is equal to 1;if M is a metal having seven coordination sites and L′ is bidentate,then a is equal to 2.

The following preferably applies to the compounds of the formulae (16)to (18):

If M is a metal having six coordination sites, then a is equal to 0;

if M is a metal having seven coordination sites and L′ is monodentate,then a is equal to 1if M is a metal having eight coordination sites and L′ is monodentate,then a is equal to 2;if M is a metal having eight coordination sites and L′ is bidentate,then a is equal to 1.

In a further embodiment of the present invention, it is preferred for Min the structural unit of the general formula (13) to (21) to be a metalhaving four, six or eight coordination sites.

The index m in the structural unit of the general formula (13) to (21)is preferably equal to 1 or 2.

In still a further embodiment of the present invention, the furtherstructural unit and the still further structural unit in the compound,oligomer or polymer in accordance with the above-mentioned embodimentsis in each case, independently of one another, a structural unit whichinclude a metal and/or a mono- or bidentate ligand. The further andstill further structural unit may be identical or different from oneanother. The further structural unit and the still further structuralunit is particularly preferably in each case, independently of oneanother, a structural unit of the formula (13) to (21). The further andstill further structural unit is extraordinarily preferably a structuralunit of the same formula as the structural unit according to theinvention. In this case, the oligomer or polymer is a homopolymer.

If the structural unit of the general formula (13) to (21) in thecompound, oligomer or polymer in accordance with the above-mentionedembodiments is a terminal structural unit in the compound, oligomer orpolymer, either a unit of the following formula (h) is bonded to L or aunit of the following formula (i) is bonded to M:

where the symbols M, L, L′, Ar, Y¹ and G and the index m have the samemeanings as in the above embodiments and the index d is equal to 0, 1,2, 3 or 4.

In a further embodiment, it is preferred for Ar in the compound of thegeneral formulae (1) to (12) or the compound, oligomer or polymer of thegeneral formulae (13) to (21) to be an aromatic or heteroaromatic ringsystem having 5 to 22 aromatic ring atoms, which may be substituted byone or more radicals R⁹. An aromatic or heteroaromatic ring system istaken to mean a ring system as defined above, which preferably has 5 to22 ring atoms. It is furthermore particularly preferred for Ar to beselected from the group consisting of phenyl, naphthalene, anthracene,phenanthrene, benzanthracene, benzophenanthrene, dibenzanthracene,pyrene, 1,3,5-triazine, pyrazine, quinoxaline and phenanthroline. Thegroups mentioned above for Ar are particularly preferred.

In still a further embodiment, it is preferred for Y¹ and Y² in thecompound of the general formulae (1) to (12) or the compound, oligomeror polymer of the general formulae (13) to (21) in each case,independently of one another, either not to be present or to representan aromatic or heteroaromatic ring system having 5 to 10 aromatic ringatoms. Y¹ and Y² are particularly preferably each selected,independently of one another, from the group consisting of a singlecovalent bond, phenyl, naphthalene, anthracene and thiophene. The groupsmentioned above for Y¹ and Y² are particularly preferred.

The group W in the embodiments according to the invention is preferablyan oxygen atom.

The group L′ is preferably a monodentate or bidentate ligand. Examplesof monodentate ligands L′ include the following structures (1) to (26):

Structures (1) to (23) coordinate here via the oxygen and structures(24) to (26) via the silicon.

L′ is preferably a bidentate ligand. L′ is particularly preferably equalto 8-hydroxyquinoline.

In accordance with the invention, the preferred embodiments mentionedabove can be combined with one another as desired.

Examples of suitable compounds according to the invention are compounds(1) to (160) shown below:

The present invention also relates to a ligand of the following formula(1′):

where the symbols and indices used have the same meanings as in theabove-mentioned embodiments. Above-mentioned preferred meanings arelikewise preferred here.

In a further embodiment of the present invention, the ligand of theformula (1′) is used for the preparation of a coordination compound. Tothis end, the free ligand is reacted, for example, with a correspondingmetal salt to give the complex.

Accordingly, the present invention also relates to a process for thepreparation of a compound, oligomer or polymer of the formulae (1) to(21). The compounds of the formulae (1) to (21) according to theinvention can be prepared by synthetic steps which are generally knownto the person skilled in the art. A first step involves the synthesis ofthe corresponding ligands, which are combined in a further step to givethe desired ligand system. This is followed by a reaction with thecorresponding metal, which is usually employed as a solution of asuitable metal salt, for example nBuLi/CH₃CN or AlCl₃/EtOH.

A general synthetic procedure for the preparation of the compound,oligomer or polymer of the formulae (1) to (21) is depicted in Schemes(1) and (2). The central metal M here can be replaced in analogousreactions by one of the other metals mentioned above.

The present invention additionally relates to a process for thepreparation of a ligand in which a compound of the following formula (A)is coupled to a compound of the following formula (B) by metal-catalysedSuzuki, Stille, Heck, Negishi, Sonogashira or Kumada cross-couplingreactions, giving a compound of the following formula (C):

whereA and B are each selected, independently of one another, from the groupof Br, Cl, I, O-triflate, OSO₂R¹², B(OR¹²)₂, Sn(R¹²)₃, ZnR¹², where R¹²is selected on each occurrence, independently of one another, from thegroup consisting of H, an aliphatic hydrocarbon radical having 1 to 20 Catoms and an aromatic hydrocarbon radical having 1 to 20 C atoms, andwhere two or more radicals R¹² may also form a ring system with oneanother;P is a hydroxyl-protecting group; and the other symbols and indices havethe same meanings as in the above embodiments.

Examples of the hydroxyl-protecting group P are methyl,t-butoxycarbonyl, benzyl, tri-t-butylsilyl ether, t-butyldimethylsilylether, t-butyldiphenhylsilyl ether and trimethylsilyl ether.

A general synthetic procedure for the preparation of compounds of theformula (C) according to the invention is depicted in Scheme (3).

In the case where two radicals R¹² can form a ring system, these twolinked radicals R¹² preferably represent a divalent aliphatic grouphaving 2 to 8 carbon atoms. Examples thereof are compounds of thefollowing formula —CH₂(CH₂)_(n)CH₂—, where n=0, 1, 2, 3, 4, 5 or 6,where n=0, 1, 2 or 3 is preferred. In the case where more than tworadicals R¹² form a ring system with one another, these radicals R¹²represent with one another a branched tri-, tetra-, penta- or polyvalentaliphatic group having 6 to 20 carbon atoms.

The present invention also relates to a process for the preparation of acompound of the following formula (B) in which a compound of thefollowing formula (D) is reacted with a compound of the followingformula (E) by, for example, metal-catalysed Suzuki, Stille, Heck,Negishi, Sonogashira, Kumada, etc., cross-coupling reactions or bynucleophilic addition onto a carbonyl group, giving a compound of thefollowing formula (C):

where

-   D is selected from the group consisting of Br, Cl, I, O-triflate,    OSO₂R¹², B(OR¹²)₂, Sn(R¹²)₃, ZnR¹², Li and MgBr;-   E is selected from the group consisting of Br, Cl, I, O-triflate,    OSO₂R¹², B(OR¹²)₂, Sn(R¹²)₃, ZnR¹², or where E, together with the C    atom to which it is bonded, forms a unit C═O;    and the other symbols and indices have the same meanings as in the    above embodiments.

A general synthetic procedure for the preparation of compounds of theformula C according to the invention is depicted in Scheme (4).

The present invention also relates to the use of a compound of theformula (C) for the preparation of a metal complex. To this end, thehydroxyl-protecting group on the compound of the formula (C) is cleavedoff, and the resultant compound of the formula (1′) is reacted, forexample, with a corresponding metal salt to give the complex.

The synthesis of a compound of the formula (1) is depicted by way ofexample in Scheme 5.

The synthesis of a compound of the formula (X) is shown by way ofexample in Scheme 6: 2-bromoanthraquinone is converted into thecorresponding bromobis(hydroxyquinoline) derivative by reaction with ahydroxy-quinolinemagnesium bromide derivative and subsequent reductionusing SnCl₂. This product is subsequently converted into thecorresponding boronic ester. The resultant compound is reacted with2,4-diphenyl-1,3,5-triazine by Suzuki coupling. After deprotection ofthe hydroxyl groups, the compound is reacted with n-BuLi to give thecompound according to the invention.

Instead of the phenyl derivative and anthracenyl derivative, all othercompounds having various aromatic skeletons and bondednitrogen-containing heterocycles (for example pyridine, pyrimidine,triazine, benzimidazole) can be prepared analogously thereto.

The invention also relates to the use of the compounds according to theinvention in an electronic device, in particular as electron-transportmaterial. In accordance with the invention, the electronic device canbe, for example, organic electroluminescent devices (OLEDs) or polymericelectroluminescent devices (PLEDs), organic integrated circuits (O-ICs),organic field-effect transistors (O-FETs), organic thin-film transistors(O-TFTs), organic light-emitting transistors (O-LETs), organic solarcells (O-SCs), organic optical detectors, organic photoreceptors,organic field-quench devices (O-FQDs), light-emitting electrochemicalcells (LECs) or organic laser diodes (O-lasers), but in particularorganic electroluminescent devices (OLEDs, PLEDs).

The invention also relates to the use of the compounds according to theinvention as charge-transport material and/or charge-injection material,preferably in a corresponding layer. These are, in particular,electron-transport layers or electron-injection layers. The use ascharge-blocking material is also possible.

The invention likewise relates to electronic devices, such as, forexample, organic electroluminescent devices or polymericelectroluminescent devices (OLEDs, PLEDs), organic integrated circuits(O-ICs), organic field-effect transistors (O-FETs), organic thin-filmtransistors (O-TFTs), organic light-emitting transistors (O-LETs),organic solar cells (O-SCs), organic optical detectors, organicphotoreceptors, organic field-quench devices (O-FQDs), light-emittingelectrochemical cells (LECs) or organic laser diodes (O-lasers), but inparticular organic electroluminescent devices (organic light-emittingdiodes, OLEDs, PLEDs), comprising one or more compounds, oligomers orpolymers of the formulae (1) to (21), as defined above. The electronicdevice here comprises anode, cathode and at least one layer whichcomprises at least one organic or organometallic compound. However, thedevice may also comprise inorganic materials.

The compound, oligomer or polymer of the formulae (1) to (21) ispreferably present within one layer in the electronic device.

The invention thus also relates to a layer comprising at least onecompound, oligomer or polymer of the formulae (1) to (21), as definedabove.

The organic electroluminescent device comprises cathode, anode and atleast one emitting layer. Apart from these layers, it may also comprisefurther layers, for example in each case one or more hole-injectionlayers, hole-transport layers, hole-blocking layers, electron-transportlayers, electron-injection layers, exciton-blocking layers and/orcharge-generation layers. Interlayers, which have, for example, anexciton-blocking function, may likewise be introduced between twoemitting layers. However, it should be pointed out that each of theselayers does not necessarily have to be present. These layers maycomprise a compound, oligomer or polymer of the formulae (1) to (21), asdefined above.

In a preferred embodiment of the invention, the compound, oligomer orpolymer of the formulae (1) to (21) is employed as compound in anelectron-transporting layer. The organic electroluminescent device heremay comprise one electron-transporting layer or it may comprise aplurality of electron-transporting layers, where at least oneelectron-transporting layer comprises at least one compound, oligomer orpolymer of the formulae (1) to (21), as defined above. The device mayfurthermore comprise further charge-transport layers and emittinglayers.

Preference is furthermore given to an organic electroluminescent devicein which one or more layers are applied by means of a sublimationprocess, in which the materials are applied by vapour deposition invacuum sublimation units at an initial pressure of less than 10⁻⁵ mbar,preferably less than 10⁻⁶ mbar. It is also possible for the initialpressure to be even lower, for example less than 10⁻⁷ mbar.

Preference is likewise given to an organic electroluminescent device,characterised in that one or more layers are applied by means of theOVPD (organic vapour phase deposition) process or with the aid ofcarrier-gas sublimation, in which the materials are applied at apressure between 10⁻⁵ mbar and 1 bar. A special case of this process isthe OVJP (organic vapour jet printing) process, in which the materialsare applied directly through a nozzle and thus structured (for exampleM. S. Arnold et al., Appl. Phys. Lett. 2008, 92, 053301).

Preference is furthermore given to an organic electroluminescent device,characterised in that one or more layers are produced from solution,such as, for example, by spin coating, or by means of any desiredprinting process, such as, for example, screen printing, flexographicprinting, offset printing, LITI (light induced thermal imaging, thermaltransfer printing), inkjet printing or nozzle printing. Solublecompounds, which are obtained, for example, by suitable substitution,are necessary for this purpose. Since the compounds according to theinvention have high solubility in organic solvents, they areparticularly suitable for processing from solution.

These processes are generally known to the person skilled in the art andcan be applied by him without problems to organic electroluminescentdevices comprising a compound, oligomer or polymer of the formulae (1)to (21), as defined above.

The invention furthermore relates to a formulation or solutioncomprising at least one compound of the formula (1) to (21) and at leastone solvent, preferably an organic solvent.

The compounds according to the invention described above, in particularcompounds which are substituted by reactive groups or arefunctionalised, can be used as monomers for the generation ofcorresponding oligomers, dendrimers or polymers.

The compounds according to the invention and the organicelectroluminescent devices produced therewith are distinguished by thefollowing surprising advantages compared with the prior art:

-   -   The compounds according to the invention have high solubility        and can therefore be processed very well from solution.    -   Organic electroluminescent devices comprising a compound,        oligomer or polymer of the formulae (1) to (21) as        electron-transport materials have an excellent lifetime.    -   On use of the compounds according to the invention as        electron-transport materials, it is not necessary to use a        separate electron-injection layer or to dope the        electron-transport layer with a further electron-injection        material. This represents an advantage in the production of the        OLED.    -   The compounds according to the invention, employed in organic        electroluminescent devices, result in high efficiencies and in        steep current/voltage curves at the same time as a low use        voltage.

These above-mentioned advantages are not accompanied by an impairment ofthe other electronic properties.

The invention is explained in greater detail by the following examples,without wishing to restrict it thereby. The person skilled in the artwill be able to synthesise further compounds according to the inventionwithout inventive step and employ them in organic electroluminescentdevices.

EXAMPLES

The following syntheses are carried out, unless indicated otherwise,under a protective-gas atmosphere in dried solvents.

8-Hydroxyquinoline can be halogenated in the 5-position in accordancewith Synthesis, 2006, 8 1325 or Chem. Eur. J., 2005, 11, 6818, and thehydroxyl group can subsequently be protected as silyl ether.

4-Bromobenzaldehyde can be converted into the correspondingbromo-benzimidazole derivative by reaction withN-phenyl-o-phenylenediamine in the presence of Oxone®, and this issubsequently converted into the corresponding boronic ester:

The resultant compound is reacted with the iodohydroxyquinolinederivative by Suzuki coupling. After deprotection of the hydroxyl group,the compound is reacted with n-BuLi to give the compound according tothe invention.

Example 1 Synthesis of lithium5-[4-(1-phenyl-1H-benzimidazol-2-yl)-phenyl]-8-hydroxyquinolate

a) 8-Hydroxy-5-iodoquinoline

A solution of 8-hydroxyquinoline (25.0 g, 172.3 mmol), NaI (26.0 g,172.5 mmol) and NaOH (6.9 g, 172.5 mmol) in MeOH (750 ml) is degassed bypassing-through of N₂ for 60 min. at room temperature. After cooling to−30° C., a 5% aqueous NaOCl solution (250 ml) is added dropwise. Themixture is stirred vigorously at −30° C. for 30 min. and thenneutralised using a 10% aqueous HCl solution. The precipitated productis filtered off. After two recrystallisations from MeOH/heptane (1:1,v/v), a pale-yellow solid is obtained (14 g, 27%).

b) 8-(tert-Butyldimethylsilyloxy)-5-iodoquinoline

8-Hydroxy-5-iodoquinoline (7.0 g, 25.8 mmol), imidazole (1.85 g, 27.2mmol) and tert-butyldimethylsilyl chloride (4.28 g, 28.4 mmol) aredissolved in anhydrous CH₂Cl₂ (40 ml) under N₂. The mixture is stirredvigorously overnight, then diluted with CH₂Cl₂ (60 ml) and washed with5% aqueous HCl (2×30 ml) and water (40 ml). The organic phase is driedover sodium sulfate, and the solvent is distilled off under reducedpressure, leaving a brown liquid. This crude product is purified byflash chromatography on silica (heptane:ethyl acetate 5:1). The endproduct is isolated as pale-yellow solid (8 g, 80%).

c) 2-(4-Bromophenyl)-1-phenyl-1H-benzimidazole

N-Phenyl-o-phenylenediamine (50 g, 0.27 mol) is dissolved in anhydrousDMF (400 ml) under N₂, and 4-bromobenzaldehyde (45.5 g, 0.25 mol) isadded dropwise. The reaction mixture is warmed to 40° C., and Oxone(potassium hydrogen monopersulfate, 98.1 g, 0.16 mol) is added inportions. After the mixture has been stirred at room temperature for 120min., 1 l of water is added. The precipitated product is filtered off,washed with water and dried in vacuo. Recrystallisation fromacetonitrile gives a cream-coloured solid (31 g, 35%).

d)1-Phenyl-244-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1H-benzimidazole

A mixture of 2-(4-bromophenyl)-1-phenyl-1H-benzimidazole (20.0 g, 57mmol), bis(pinacolato)diboron (16.0 g, 63 mmol), potassium acetate (18.6g, 0.19 mol), PdCl₂(dppf)×CH₂Cl₂ (0.75 g, 1 mmol) and dioxane (360 ml)is degassed for 30 min. The reaction mixture is heated under reflux for6 h. After cooling to room temperature, the mixture is poured intoice-water (80 ml) and extracted with toluene. The combined organicphases are dried over sodium sulfate, and the solvent is distilled offunder reduced pressure, leaving a brown liquid. The end product isisolated as pale-brown solid (22.8 g, 97%).

e)8-(tert-Butyldimethylsilanyloxy)-5-[4-(1-phenyl-1H-benzimidazol-2-yl)phenyl]quinoline

A mixture of1-phenyl-2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-phenyl]-1H-benzimidazole(8.9 g, 22.4 mmol), 8-(tert-butyldimethylsilyl-oxy)-5-iodoquinoline (7.2g, 18.69 mmol), toluene (110 ml) and dioxane (110 ml) is degassed bypassing through of N₂ for 30 min. Pd(OAc)₂ (9 mg, 0.04 mmol) andtris-o-tolylphosphine (75.6 mg, 0.25 mmol) is then added, and themixture is heated at 80° C. for 8 h. After cooling to room temperature,the mixture is diluted with water (100 ml) and extracted with ethylacetate (3×50 ml). The combined organic phases are dried over sodiumsulfate, and the solvent is removed under reduced pressure. The crudeproduct is purified by flash chromatography on silica andcrystallisation (7.9 g, 80%).

f) 544-(1-Phenyl-1H-benzimidazol-2-yl)phenyl]quinolin-8-ol

A 1M TBAF solution in THF (22.4 ml, 22.4 mmol) is added dropwise to asolution of8-(tert-butyldimethylsilanyloxy)-544-(1-phenyl-1H-benzimidazol-2-yl)phenyl]quinoline(7.9 g, 14.90 mmol) in THF (20 ml). After stirring for 4 h, the mixtureis washed with 5% aqueous NH₄Cl (100 ml) solution and extracted withethyl acetate (3×50 ml). The combined organic phases are dried oversodium sulfate, and the solvent is removed under reduced pressure. Thecrude product is purified by flash chromatography on silica andcrystallisation from MeOH (5.9 g, 90%).

g) Lithium5-[4-(1-phenyl-1H-benzimidazol-2-yl)phenyl]-8-hydroxy-quinolate

5-[4-(1-Phenyl-1H-benzimidazol-2-yl)phenyl]quinolin-8-ol (2.1 g, 4.8mmol) is dissolved in acetonitrile (100 ml), and 2.5 M n-butyllithium(1.9 ml, 4.8 mmol) is added. The solution is stirred at room temperaturefor 1 h. The yellow precipitate is filtered off, washed withacetonitrile and dried in vacuo (1.9 g, 94%).

Example 2 Synthesis of lithium5,5′12-(9,10-anthracen-2-yl)-4,6-diphenyl-1,3,5-triazinyl]bis-8-quinolinate

a)5,5′-(2-Bromoanthracene-9,10-diyl)-8-(tert-butyldimethylsilanyloxy)-bisquinoline

Magnesium (2.3 g, 97 mmol) is initially introduced in 50 ml of dry THF.A solution of 5-bromo-8-hydroxyquinoline (20 g, 89 mmol) in 400 ml ofdry THF is added dropwise, the mixture is stirred at 70° C. for 2 h,then allowed to come to room temperature. The resultant Grignard reagentis added dropwise, with ice-cooling, to 2-bromo-9,10-anthraquinone (25.5g, 89 mmol) in 200 ml of dry THF. After 4 h with ice-cooling, 200 ml ofsaturated NH₄Cl solution are slowly added dropwise, the mixture isextracted with ethyl acetate, the organic phase is dried over Na₂SO₄ andevaporated in a rotary evaporator. The reaction mixture (52 g) issuspended in DMF (400 ml), tin chloride (67.5 g, 356 mmol) is added, andthe mixture is heated to 140° C. 300 ml of EtOH are added, then 50 ml of2M HCL are added dropwise. The solid is filtered off, washed with EtOHand dried in vacuo (38.2 g, 51%).

b)Bis-(8-(tert-butyldimethysilanyloxyquinolin-5-yl)-9,10-anthracenyl)-2-boronicacid

39.3 g (51 mmol) of the bromide from a) are dissolved in 600 ml of dryTHF and cooled to −78° C. 26.2 ml (65.7 mmol/2.5 M in hexane) ofn-butyllithium are added over the course of about 5 min. at thistemperature, and the mixture is subsequently stirred at −78° C. for afurther 2.5 h. 7.3 ml (65.7 mmol) of trimethyl borate are added asrapidly as possible at this temperature, and the reaction is allowed tocome slowly to RT (about 18 h). The reaction solution is washed withwater, and the precipitated solid and the organic phase are driedazeotropically with toluene. The crude product is washed by stirringwith toluene/methylene chloride at about 40° C. and filtered off withsuction, giving 30.1 g (80%) of the product as white solid.

c)5,5′-(2-(4,6-Diphenyl-1,3,5-triazinyl)anthracene-9,10-diyl)-8-(tert-butyldimethylsilanyloxy)bisquinoline

34.4 g (46.8 mmol) of the boronic acid from b), 11.3 g (42.15 mmol) of2-chloro-4,6-diphenyl-1,3,5-triazine and 9.9 g of sodium carbonate aresuspended in 300 ml of dioxane, 300 ml of toluene and 100 ml of water.2.7 g (2.3 mmol) of Pd(PPh₃)₄ are added to this suspension. The reactionmixture is heated under reflux for 7 h. After cooling, the precipitatedsolid is filtered off with suction, washed with water and ethanol anddried. The residue is extracted with hot toluene and recrystallised fromtoluene. Yield: 27.2 g, 70% of theory

d)5,5′-[2-(4,6-Diphenyl-1,3,5-triazinyl)anthracene-9,10-diyl)bis-quinolin-8-ol

A 1M TBAF solution in THF (22.4 ml, 22.4 mmol) is added dropwise to asolution of5,5′-(2-(4,6-diphenyl-1,3,5-triazinyl)anthracene-9,10-diyl)-8-(tert-butyldimethylsilanyloxy)bisquinoline(13.76 g, 14.90 mmol) in THF (20 ml). After stirring for 4 h, themixture is washed with 5% aqueous NH₄Cl solution (100 ml) and extractedwith ethyl acetate. The combined organic phases are dried over sodiumsulfate, and the solvent is removed under reduced pressure. The crudeproduct is purified by flash chromatography on silica and withcrystallisation from MeOH (9.25 g, 90%).

e) Lithium5,5′42-(4,6-diphenyl-1,3,5-triazinyl)-(9,10-anthracenediyl)]-bis-8-quinolinolate

5,5′-[2-(4,6-Diphenyl-1,3,5-triazinyl)anthracene-9,10-diyl)bisquinolin-8-ol(6.95 g, 10 mmol) is dissolved in acetonitrile (300 ml), and 2.5 Mn-butyl-lithium (9.9 ml, 25 mmol) is added. The solution is stirred atroom temperature for 1 h. The yellow precipitate is filtered off, washedwith acetonitrile and dried in vacuo (5.8 g, 80%).

Example 3 Production of OLEDs

OLEDs according to the invention and OLEDs in accordance with the priorart are produced by a general process in accordance with WO 2004/058911,which is adapted to the circumstances described here (layer-thicknessvariation, materials used).

The results for various OLEDs are presented in Examples 4 to 23 below(see Table 1 and 2). Glass plates coated with structured ITO (indium tinoxide) in a thickness of 150 nm are coated with 20 nm of PEDOT(poly(3,4-ethylenedioxy-2,5-thiophene), spin-coated from water;purchased from H. C. Starck, Goslar, Germany) for improved processing.These coated glass plates form the substrates to which the OLEDs areapplied. The OLEDs have the following layer structure: substrateITO/hole-transport layer (HTL 140 nm)/interlayer (IL 5nm)/electron-blocking layer (EBL 20 nm)/emission layer (EML (H1 or H2+x% by vol. of D1 or D2) z nm)/electron-transport layer (ETL ynm)/optional electron-injection layer (EIL 1 nm) and finally a cathode.The cathode is formed by an aluminium layer with a thickness of 100 nm.The precise structure of the OLEDs is shown in Table 1. The materialsused for the production of the OLEDs are shown in Table 3.

All materials are applied by thermal vapour deposition in a vacuumchamber. The emission layer here always consists of at least one matrixmaterial (=host material) and an emitting dopant (=emitter), which isadmixed with the matrix material or the matrix materials in a certainproportion by volume by co-evaporation. An indication such as H1:D1(95%:5%) here means that material H1 is present in the layer in aproportion by volume of 95% and D1 is present in the layer in aproportion by volume of 5%. The electron-transport layer can alsoconsist analogously of a mixture of two materials.

The OLEDs are characterised by standard methods. For this purpose, theelectroluminescence spectra, current/voltage/luminance characteristiclines (IUL characteristic lines) and the lifetime are measured. Thelifetime is defined as the time after which the luminous density hasdropped to a certain proportion from a certain initial luminous densityI₀. The indication LD50 means that the said lifetime is the time atwhich the luminous density has dropped to 0.5·I₀ (to 50%), i.e. from,for example, 6000 cd/m² to 3000 cd/m². The current efficiency (cd/A) andthe power efficiency (Im/W) are calculated from the IUL characteristiclines.

The compounds according to the invention can be employed, inter alia, aselectron-transport material for fluorescent and phosphorescent OLEDs.Compounds ETM2, ETM3 and ETM4 according to the invention are used here.The comparison in accordance with the prior art used is compound ETM1.The results for the OLEDs are summarised in Table 2. Ex. 1-9 show OLEDscomprising materials in accordance with the prior art and serve ascomparative examples. The OLEDs according to the invention in Ex. 10-23exhibit the advantages on use of compounds of the formula (1) accordingto the invention. The use of compounds according to the inventionenables improvements to be achieved, compared with the prior art, in theoperating voltage, efficiency and lifetime of the components

Compared with the reference components, the electrical characteristicdata are in all cases comparable or better. With an otherwise identicallayer structure, the components according to the invention exhibitimproved performance data.

TABLE 1 Structure of the OLEDs Ex. EML ETL EIL 4 (comp.) H1:D1 ETM1 —(95%:5%)  20 nm 30 nm 5 (comp.) H1:D1 ETM1 EIL1 (95%:5%)  20 nm 1 nm 30nm 6 (comp.) H1:D1 ETM1:EIL1 — (95%:5%)  (50:50) 30 nm 20 nm 7 (comp.)H2:D2 ETM1 — (85%:15%) 30 nm 40 nm 8 (comp.) H2:D2 ETM1 EIL1 (85%:15%)30 nm 1 nm 40 nm 9 (comp.) H2:D2 ETM1:EIL1 — (85%:15%) (50:50) 40 nm 30nm 10 H1:D1 ETM2 — (95%:5%)  20 nm 30 nm 11 H1:D1 ETM3 — (95%:5%)  20 nm30 nm 12 H1:D1 ETM4 — (95%:5%)  20 nm 30 nm 13 H1:D1 ETM1 ETM2 (95%:5%) 20 nm 30 nm 14 H1:D1 ETM1 ETM3 (95%:5%)  20 nm 30 nm 15 H1:D1 ETM1:EMT3(95%:5%)  (50:50) 30 nm 20 nm 16 H1:D1 ETM1:ETM4 (95%:5%)  (50:50) 30 nm20 nm 17 H2:D2 ETM2 — (85%:15%) 20 nm 40 nm 18 H2:D2 ETM3 — (85%:15%) 20nm 40 nm 19 H2:D2 ETM4 — (85%:15%) 20 nm 40 nm 20 H2:D2 ETM1 ETM2(85%:15%) 20 nm 40 nm 21 H2:D2 ETM1 ETM3 (85%:15%) 20 nm 40 nm 22 H2:D2ETM1:EMT3 (85%:15%) (50:50) 40 nm 20 nm 23 H2:D2 ETM1:ETM4 (85%:15%)(50:50) 40 nm 20 nm

TABLE 2 Results for the OLEDs Voltage Efficiency LD50 [V] for [cd/A] atCIE x/y at I₀ = Ex. 1000 cd/m2 1000 cd/m2 1000 cd/m² 6000 cd/m² 4(comp.) 7.5 4.3 0.146 0.167 50 10 4.4 8.1 0.143 0.161 130 11 4.8 7.40.143 0.162 100 12 4.0 8.3 0.141 0.160 160 5 (comp.) 4.4 7.8 0.142 0.160160 13 4.3 8.1 0.142 0.161 180 14 4.0 8.3 0.142 0.161 210 6 (comp.) 4.37.9 0.142 0.162 230 15 3.9 8.6 0.143 0.161 260 16 4.0 8.8 0.143 0.162280 7 (comp.) 7.1 14.8 0.34 0.58 110 17 4.8 36.3 0.35 0.61 280 18 4.642.4 0.35 0.61 360 19 3.9 46.5 0.35 0.61 380 8 (comp.) 3.8 39.3 0.350.60 670 20 3.7 40.1 0.35 0.60 750 21 3.6 40.6 0.35 0.60 780 9 (comp.)3.7 42.5 0.35 0.61 860 22 3.8 45.3 0.35 0.61 950 23 3.5 48.7 0.35 0.611030

TABLE 3 Structural formulae of the materials used

IL

HTL

EBL

ETM1

EIL1

H1

D1

H2

D2

ETM2

ETM3

ETM4

1-16. (canceled)
 17. A compound of the general formula (1) or (2),

where the symbols and indices used have the following meanings: G is,identically or differently on each occurrence, a group of the followingformula (a), (b) or (c):

Q is, identically or differently on each occurrence, a N or CR³, V isselected from the group consisting of O, S, N, CR⁴ and NR⁴, with theproviso that, if V is equal to O, S or NR⁴, R³ represents a non-bondingelectron pair; the two dashed bonds in formula (a) and (b) mean that oneof the bonds is a single covalent bond and the other is a doublecovalent bond; R¹ is selected identically or differently on eachoccurrence, from the group defined for R², R³ or R⁴; where one R¹ is notpresent, and the quinoline unit is bonded to Y² at this position; R², R³and R⁴ are, identically or differently on each occurrence, a H, D, F,Cl, Br, I, CHO, N(Ar¹)₂, C(═O)Ar¹, P(═O)(Ar¹)₂, S(═O)Ar¹, S(═O)₂Ar¹,CR⁵═CR⁵Ar¹, CN, NO₂, Si(R⁵)₃, B(OAr¹)₂, B(OR⁵)₂, OSO₂R⁵, OH, a saturatedor unsaturated, straight-chain, branched or cyclic C₁₋₄₀-alkyl group,C₁₋₄₀-alkoxy group or C₁₋₄₀-thioalkyl group, each of which is optionallysubstituted by one or more radicals R⁵, where one or more non-adjacentCH₂ groups is optionally replaced by R⁵C═CR⁵, C≡C, Si(R⁵)₂, Ge(R⁵)₂,Sn(R⁵)₂, C═O, C═S, C═Se, C═NR⁵, P(═O)(R⁵), SO, SO₂, NR⁵, O, S or CONR⁵,and where one or more H atoms is optionally replaced by D, F, Cl, Br, I,CN or NO₂, an aromatic or heteroaromatic ring system having 5 to 60aromatic ring atoms, which is optionally substituted by one or moreradicals R⁶, an aryloxy or heteroaryloxy group having 5 to 60 aromaticring atoms, which is optionally substituted by one or more radicals R⁶,and a combination of these systems; where one of the substituents R², R³or R⁴ is not present on the group G, and the group G is bonded to Y¹ atthis position; W is, identically or differently on each occurrence, anO, S or NR⁸, where R⁸ is selected from the group defined for R², R³ orR⁴; Y¹ and Y² are each, independently of one another, either notpresent, so that the groups bonded thereto are linked directly to oneanother by a single covalent bond, or are a saturated or unsaturated,linear, branched or cyclic C₁₋₄₀-alkyl group or an aromatic orheteroaromatic ring system having 5 to 60 ring atoms, which isoptionally substituted by one or more radicals R⁶; Ar is an aromatic orheteroaromatic ring system having 5 to 60 aromatic ring atoms, which isoptionally substituted by one or more radicals R⁹, where R⁹ is selectedfrom the group defined for R², R³ or R⁴; Ar¹ is, identically ordifferently on each occurrence, an aromatic or heteroaromatic ringsystem having 5 to 30 aromatic ring atoms, which is optionallysubstituted by one or more radicals R⁷, where, in addition, two radicalsAr¹ which are bonded to the same nitrogen or phosphorus atom isoptionally linked to one another by a single bond or a bridge selectedfrom the group consisting of B(R⁷), C(R⁷)₂, Si(R⁷)₂, C═O, C═NR⁷,C═C(R⁷)₂, O, S, S═O, SO₂, N(R⁷), P(R⁷) and P(═O)R⁷; R⁵ is, identicallyor differently on each occurrence, a H, D, a saturated or unsaturated,linear, branched or cyclic C₁₋₂₀-alkyl group, in which one or more Hatoms is optionally replaced by D or F, or an aromatic or heteroaromaticring system having 5 to 20 ring atoms, in which one or more H atoms isoptionally replaced by F, and which is optionally substituted by one ormore radicals R⁶; R⁶ is, identically or differently on each occurrence,a H, D, F, Cl, Br, I, CHO, N(Ar¹)₂, C(═O)Ar¹, P(═O)(Ar¹)₂, S(═O)Ar¹,S(═O)₂Ar¹, CR⁷═CR⁷Ar¹, CN, NO₂, Si(R⁷)₃, B(OAr¹)₂, B(OR⁷)₂, OSO₂R⁷, OH,or a saturated or unsaturated, straight-chain, branched or cyclicC₁₋₄₀-alkyl group, C₁₋₄₀-alkoxy group or C₁₋₄₀-thioalkyl group, each ofwhich is optionally substituted by one or more radicals R⁷, where one ormore non-adjacent CH₂ groups is optionally replaced by R⁷C═CR⁷, C≡C,Si(R⁷)₂, Ge(R⁷)₂, Sn(R⁷)₂, C═O, C═S, C═Se, C═NR⁷, P(═O)(R⁷), SO, SO₂,NR⁷, O, S or CONR⁷, and where one or more H atoms is optionally replacedby D, F, Cl, Br, I, CN or NO₂; R⁷ is identically or differently on eachoccurrence, a H, D, a saturated or unsaturated, linear, branched orcyclic C₁₋₂₀-alkyl group, in which one or more H atoms is optionallyreplaced by F or D, and an aromatic or heteroaromatic ring system having5 to 20 ring atoms, in which one or more H atoms is optionally replacedby F or D; M is, identically or differently on each occurrence, a mono-,di-, tri- or tetravalent metal; L′ is, identically or differently oneach occurrence, a monodentate or bidentate ligand; m is, identically ordifferently on each occurrence, 0, 1, 2, 3 or 4, with the proviso thatat least one index m is >0; n is 1, 2, 3 or 4; r is 1, 2, 3 or 4; k is,identically or differently on each occurrence, 0, 1, 2, 3, 4, 5 or 6;and l is 0, 1, 2, 3, 4, 5 or
 6. 18. The compound according to claim 17,wherein M is an element, a metal or a metal ion selected from the groupconsisting of Li, Be, Ca, Mg, Ba, Zn, B, Al, Zr, Cu, Sc and Y.
 19. Thecompound according to claim 17, wherein M is an element, a metal or ametal ion is Li, Al or Zr.
 20. The compound according to claim 17,wherein the following applies to compounds of the formula (I): if M is ametal having two coordination sites, then k is equal to 0; if M is ametal having three coordination sites and L′ is a monodentate ligand,then k is equal to 1; if M is a metal having four coordination sites andL′ is a monodentate ligand, then k is equal to 2; if M is a metal havingfive coordination sites and L′ is a monodentate ligand, then k is equalto 3; if M is a metal having six coordination sites and L′ is amonodentate ligand, then k is equal to 4; if M is a metal having sevencoordination sites and L′ is a monodentate ligand, then k is equal to 5;if M is a metal having eight coordination sites and L′ is a monodentateligand, then k is equal to 6; if M is a metal having four coordinationsites and L′ is a bidentate ligand, then k is equal to 1; if M is ametal having six coordination sites and L′ is a bidentate ligand, then kis equal to 2; if M is a metal having eight coordination sites and L′ isa bidentate ligand, then k is equal to 3; and wherein the followingapplies to compounds of the formula (II): if M is a metal having twocoordination sites and r is equal to 1, then l is equal to 0; if M is ametal having three coordination sites, L′ is a monodentate ligand and ris equal to 1, then l is equal to 1; if M is a metal having fourcoordination sites, L′ is a monodentate ligand and r is equal to 1, thenl is equal to 2; if M is a metal having five coordination sites, L′ is amonodentate ligand and r is equal to 1, then l is equal to 3; if M is ametal having six coordination sites, L′ is a monodentate ligand and r isequal to 1, then l is equal to 4; if M is a metal having sevencoordination sites, L′ is a monodentate ligand and r is equal to 1, thenl is equal to 5; if M is a metal having eight coordination sites, L′ isa monodentate ligand and r is equal to 1, then l is equal to 6; if M isa metal having four coordination sites and r is equal to 2, then l isequal to 0; if M is a metal having five coordination sites, L′ is amonodentate ligand and r is equal to 2, then l is equal to 1; if M is ametal having six coordination sites, L′ is a monodentate ligand and r isequal to 2, then l is equal to 2; if M is a metal having sevencoordination sites, L′ is a monodentate ligand and r is equal to 2, thenl is equal to 3; if M is a metal having eight coordination sites, L′ isa monodentate ligand and r is equal to 2, then l is equal to 4; if M isa metal having six coordination sites and r is equal to 3, then l isequal to 0; if M is a metal having seven coordination sites, L′ is amonodentate ligand and r is equal to 3, then l is equal to 1; if M is ametal having eight coordination sites, L′ is a monodentate ligand and ris equal to 3, then l is equal to 2; if M is a metal having eightcoordination sites and r is equal to 4, then l is equal to 0; if M is ametal having four coordination sites, L′ is a bidentate ligand and r isequal to 1, then l is equal to 1; if M is a metal having sixcoordination sites, L′ is a bidentate ligand and r is equal to 1, then lis equal to 2; if M is a metal having eight coordination sites, L′ is abidentate ligand and r is equal to 1, then l is equal to 3; if M is ametal having six coordination sites, L′ is a bidentate ligand and r isequal to 2, then l is equal to 1; if M is a metal having eightcoordination sites, L′ is a bidentate ligand and r is equal to 2, then lis equal to 2; if M a metal having eight coordination sites, L′ abidentate ligand and r equal to 3, then l is equal to 1; if M a metalhaving eight coordination sites, L′ bidentate ligand and r equal to 4,then l is equal to
 0. 21. The compound according to claim 17, whereinthe group Ar is selected from the following formulae, each of which mayalso be substituted by one or more radicals R⁹:


22. The compound according to claim 17, wherein the group G is selectedfrom the following formulae, each of which may also be substituted byone or more substituents R², R³ or R⁴:


23. The compound according to claim 17, wherein the groups Y¹ and Y²,identically or differently on each occurrence, are not present or areselected from the following groups, each of which may also besubstituted by one or more substituents R⁶:


24. The compound according to claim 17, selected from the compounds ofthe formulae (3) to (12):

where the symbols used have the following meanings: Y¹, Y² have the samemeaning as defined in claim 17; R¹⁰ is, identically or differently oneach occurrence, either H or a radical of the following formula (d):

where L′, k and R¹ have the same meanings as defined in claim 17, withthe proviso that one R¹ is not present, and the compound of the formula(d) is bonded to the compound of the formula (3) to (12) at thisposition; R¹¹ is, identically or differently on each occurrence, eitherH or a radical of the following formula (e) or (f):

where V is selected from the group consisting of O, S and NR⁴ and Q isselected from the group consisting of N and CR³, where at least one Q,stand for N, and where R³ has the same meaning as defined in claim 17;with the proviso that both at least one R¹⁰ in each formula and also atleast one R¹¹ in each formula is other than H.
 25. The compoundaccording to claim 23, wherein R¹⁰ is selected from the followingformulae, where the bond drawn in indicates the position of the link toY²:


26. An oligomer or polymer which comprises the compound according toclaim 17, containing a structural unit of the general formula (13) to(21):

where the symbols Ar, L′, Y¹ and G and the index m have the samemeanings as defined in claim 17, and the other symbols and indices havethe following meanings: M is a mono-, di-, tri- or tetravalent metal; Lis a bidentate ligand of the following formula (g):

where the bond dash leading away from Y² represents a bond to Ar in thestructural units of the formulae (13) to (21), and the arrows leadingaway from W and N represent a coordination bond to M, and the symbolsY², W and R¹ have the same meanings as defined in claim 17, where one R¹is not present and the quinoline unit is bonded to Y² at this position;a is 0, 1 or 2; b is 0 or 1; with the proviso that the bond dashesleading away from L in the structural units of the formulae (13) to (21)represent a bond to M of a further structural unit, and the bond dashesleading away from M in the structural units of the formulae (13) to (21)represent a bond to L of a still further structural unit.
 27. Thecompound according to claim 17, wherein L′ is a bidentate ligand whichmay also be substituted.
 28. The compound according to claim 17, whereinL′ is a 8-hydroxyquinoline, which may also be substituted.
 29. Acompound of the following formula (1′):

wherein R¹ is selected identically or differently on each occurrence,from the group defined for R², R³ or R⁴; where one R¹ is not present,and the quinoline unit is bonded to Y² at this position; R², R³ and R⁴are, identically or differently on each occurrence, a H, D, F, Cl, Br,I, CHO, N(Ar¹)₂, C(═O)Ar¹, P(═O)(Ar¹)₂, S(═O)Ar¹, S(═O)₂Ar¹, CR⁵═CR⁵Ar¹,CN, NO₂, Si(R⁵)₃, B(OAr¹)₂, B(OR⁵)₂, OSO₂R⁵, OH, a saturated orunsaturated, straight-chain, branched or cyclic C₁₋₄₀-alkyl group,C₁₋₄₀-alkoxy group or C₁₋₄₀-thioalkyl group, each of which is optionallysubstituted by one or more radicals R⁵, where one or more non-adjacentCH₂ groups is optionally replaced by R⁵C═CR⁵, C≡C, Si(R⁵)₂, Ge(R⁵)₂,Sn(R⁵)₂, C═O, C═S, C═Se, C═NR⁵, P(═O)(R⁵), SO, SO₂, NR⁵, O, S or CONR⁵,and where one or more H atoms is optionally replaced by D, F, Cl, Br, I,CN or NO₂, an aromatic or heteroaromatic ring system having 5 to 60aromatic ring atoms, which is optionally substituted by one or moreradicals R⁶, an aryloxy or heteroaryloxy group having 5 to 60 aromaticring atoms, which is optionally substituted by one or more radicals R⁶,and a combination of these systems; where one of the substituents R², R³or R⁴ is not present on the group G, and the group G is bonded to Y¹ atthis position; W is, identically or differently on each occurrence, anO, S or NR⁸, where R⁸ is selected from the group defined for R², R³ orR⁴; Y¹ and Y² are each, independently of one another, either notpresent, so that the groups bonded thereto are linked directly to oneanother by a single covalent bond, or are a saturated or unsaturated,linear, branched or cyclic C₁₋₄₀-alkyl group or an aromatic orheteroaromatic ring system having 5 to 60 ring atoms, which isoptionally substituted by one or more radicals R⁶; Ar is an aromatic orheteroaromatic ring system having 5 to 60 aromatic ring atoms, which isoptionally substituted by one or more radicals R⁹, where R⁹ is selectedfrom the group defined for R², R³ or R⁴; Ar¹ is, identically ordifferently on each occurrence, an aromatic or heteroaromatic ringsystem having 5 to 30 aromatic ring atoms, which is optionallysubstituted by one or more radicals R⁷, where, in addition, two radicalsAr¹ which are bonded to the same nitrogen or phosphorus atom isoptionally linked to one another by a single bond or a bridge selectedfrom the group consisting of B(R⁷), C(R⁷)₂, Si(R⁷)₂, C═O, C═NR⁷,C═C(R⁷)₂, O, S, S═O, SO₂, N(R⁷), P(R⁷) and P(═O)R⁷; R⁵ is, identicallyor differently on each occurrence, a H, D, a saturated or unsaturated,linear, branched or cyclic C₁₋₂₀-alkyl group, in which one or more Hatoms is optionally replaced by D or F, or an aromatic or heteroaromaticring system having 5 to 20 ring atoms, in which one or more H atoms isoptionally replaced by F, and which is optionally substituted by one ormore radicals R⁶; R⁶ is, identically or differently on each occurrence,a H, D, F, Cl, Br, I, CHO, N(Ar¹)₂, C(═O)Ar¹, P(═O)(Ar¹)₂, S(═O)Ar¹,S(═O)₂Ar¹, CR⁷═CR⁷Ar¹, CN, NO₂, Si(R⁷)₃, B(OAr¹)₂, B(OR⁷)₂, OSO₂R⁷, OH,or a saturated or unsaturated, straight-chain, branched or cyclicC₁₋₄₀-alkyl group, C₁₋₄₀-alkoxy group or C₁₋₄₀-thioalkyl group, each ofwhich is optionally substituted by one or more radicals R⁷, where one ormore non-adjacent CH₂ groups is optionally replaced by R⁷C═CR⁷, Si(R⁷)₂,Ge(R⁷)₂, Sn(R⁷)₂, C═O, C═S, C═Se, C═NR⁷, P(═O)(R⁷), SO, SO₂, NR⁷, O, Sor CONR⁷, and where one or more H atoms is optionally replaced by D, F,Cl, Br, I, CN or NO₂; R⁷ is identically or differently on eachoccurrence, a H, D, a saturated or unsaturated, linear, branched orcyclic C₁₋₂₀-alkyl group, in which one or more H atoms is optionallyreplaced by F or D, and an aromatic or heteroaromatic ring system having5 to 20 ring atoms, in which one or more H atoms is optionally replacedby F or D; m is, identically or differently on each occurrence, 0, 1, 2,3 or 4, with the proviso that at least one index m is >0; and n is 1, 2,3 or
 4. 30. A process for the preparation of the compound according toclaim 17 which comprises reacting a compound of the formula (1′) with acompound of the metal M

wherein R¹ is selected identically or differently on each occurrence,from the group defined for R², R³ or R⁴; where one R¹ is not present,and the quinoline unit is bonded to Y² at this position; R², R³ and R⁴are, identically or differently on each occurrence, a H, D, F, Cl, Br,I, CHO, N(Ar¹)₂, C(═O)Ar¹, P(═O)(Ar¹)₂, S(═O)Ar¹, S(═O)₂Ar¹, CR⁵═CR⁵Ar¹,CN, NO₂, Si(R⁵)₃, B(OAr¹)₂, B(OR⁵)₂, OSO₂R⁵, OH, a saturated orunsaturated, straight-chain, branched or cyclic C₁₋₄₀-alkyl group,C₁₋₄₀-alkoxy group or C₁₋₄₀-thioalkyl group, each of which is optionallysubstituted by one or more radicals R⁵, where one or more non-adjacentCH₂ groups is optionally replaced by R⁵C═CR⁵, Si(R⁵)₂, Ge(R⁵)₂, Sn(R⁵)₂,C═O, C═S, C═Se, C═NR⁵, P(═O)(R⁵), SO, SO₂, NR⁵, O, S or CONR⁵, and whereone or more H atoms is optionally replaced by D, F, Cl, Br, I, CN orNO₂, an aromatic or heteroaromatic ring system having 5 to 60 aromaticring atoms, which is optionally substituted by one or more radicals R⁶,an aryloxy or heteroaryloxy group having 5 to 60 aromatic ring atoms,which is optionally substituted by one or more radicals R⁶, and acombination of these systems; where one of the substituents R², R³ or R⁴is not present on the group G, and the group G is bonded to Y¹ at thisposition; W is, identically or differently on each occurrence, an O, Sor NR^(B), where R⁸ is selected from the group defined for R², R³ or R⁴;Y¹ and Y² are each, independently of one another, either not present, sothat the groups bonded thereto are linked directly to one another by asingle covalent bond, or are a saturated or unsaturated, linear,branched or cyclic C₁₋₄₀-alkyl group or an aromatic or heteroaromaticring system having 5 to 60 ring atoms, which is optionally substitutedby one or more radicals R⁶; Ar is an aromatic or heteroaromatic ringsystem having 5 to 60 aromatic ring atoms, which is optionallysubstituted by one or more radicals R⁹, where R⁹ is selected from thegroup defined for R², R³ or R⁴; Ar¹ is, identically or differently oneach occurrence, an aromatic or heteroaromatic ring system having 5 to30 aromatic ring atoms, which is optionally substituted by one or moreradicals R⁷, where, in addition, two radicals Ar¹ which are bonded tothe same nitrogen or phosphorus atom is optionally linked to one anotherby a single bond or a bridge selected from the group consisting ofB(R⁷), C(R⁷)₂, Si(R⁷)₂, C═O, C═NR⁷, C═C(R⁷)₂, O, S, S═O, SO₂, N(R⁷),P(R⁷) and P(═O)R⁷; R⁵ is, identically or differently on each occurrence,a H, D, a saturated or unsaturated, linear, branched or cyclicC₁₋₂₀-alkyl group, in which one or more H atoms is optionally replacedby D or F, or an aromatic or heteroaromatic ring system having 5 to 20ring atoms, in which one or more H atoms is optionally replaced by F,and which is optionally substituted by one or more radicals R⁶; R⁶ is,identically or differently on each occurrence, a H, D, F, Cl, Br, I,CHO, N(Ar¹)₂, C(═O)Ar¹, P(═O)(Ar¹)₂, S(═O)Ar¹, S(═O)₂ CR⁷═CR⁷Ar¹, CN,NO₂, Si(R⁷)₃, B(OAr¹)₂, B(OR⁷)₂, OSO₂R⁷, OH, or a saturated orunsaturated, straight-chain, branched or cyclic C₁₋₄₀-alkyl group,C₁₋₄₀-alkoxy group or C₁₋₄₀-thioalkyl group, each of which is optionallysubstituted by one or more radicals R⁷, where one or more non-adjacentCH₂ groups is optionally replaced by R⁷C═CR⁷, C≡C, Si(R⁷)₂, Ge(R⁷)₂,Sn(R⁷)₂, C═S, C═Se, C═NR⁷, P(═O)(R⁷), SO, SO₂, NR⁷, O, S or CONR⁷, andwhere one or more H atoms is optionally replaced by D, F, Cl, Br, I, CNor NO₂; R⁷ is identically or differently on each occurrence, a H, D, asaturated or unsaturated, linear, branched or cyclic C₁₋₂₀-alkyl group,in which one or more H atoms is optionally replaced by F or D, and anaromatic or heteroaromatic ring system having 5 to 20 ring atoms, inwhich one or more H atoms is optionally replaced by F or D; m is,identically or differently on each occurrence, 0, 1, 2, 3 or 4, with theproviso that at least one index m is >0; and n is 1, 2, 3 or
 4. 31. Anelectronic device which comprises the compound according to claim 17.32. The electronic device as claimed in claim 31, wherein the device isan organic electroluminescent device (OLED, PLED), an organic integratedcircuit (O-IC), an organic field-effect transistor (O-FET), an organicthin-film transistor (O-TFT), an organic light-emitting transistor(O-LET), an organic solar cell (O-SC), an organic optical detector, anorganic photoreceptor, an organic field-quench device (O-FQD), alight-emitting electrochemical cell (LEC) or an organic laser diode(O-laser).
 33. An organic electroluminescent device which comprises thecompound according to claim 17 is employed in an electron-transportinglayer.
 34. A formulation comprising at least one compound according toclaim 17 and at least one solvent.